FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Infrared Forehead Thermometer (Model IR-FT)

K Number: K191668 · Decision Oct 18, 2019
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
2
Review Days
119

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Basic Information

Device Name
Infrared Forehead Thermometer (Model IR-FT)
K Number
K191668
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Comper Chuangxiang (Beijing) Technology Co., Ltd.
Date Received
June 21, 2019
Decision Date
October 18, 2019
Product Code
FLL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FLL Continuous Measurement Thermometer

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLL), ordered by most recent decision date.

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Other Clearances by Comper Chuangxiang (Beijing) Technology Co., Ltd.

K Number Device Name
K202481 ThermArt (Model IR-EFT)